Evidence map›Paper›PMID 36586284›Full record

ArticleJournal of chromatography. A2023

Computational framework for the techno-economic analysis of monoclonal antibody capture chromatography platforms.

Juan J Romero, Eleanor W Jenkins, Joshua Osuofa, Scott M Husson

Open access · greenAbstract read
In one paragraph

Article in Journal of chromatography. A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Juan J RomeroDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634 USA.
Eleanor W JenkinsSchool of Mathematical and Statistical Sciences, Clemson University, Clemson, SC 29634 USA.
Joshua OsuofaDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634 USA.
Scott M HussonDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634 USA. Electronic address: shusson@clemson.edu.
Clemson University · US

Funding

Strategies for continuous biologics purification with new affinity membranesR15GM131341 · NIGMS · CLEMSON UNIVERSITY · PI HUSSON, SCOTT M · 2018 to 2018
$422k
NIGMS NIH HHS R15 GM131341
6 · The paper itself

Abstract

We developed a computational framework that integrates commercial software components to perform customizable technoeconomic feasibility analyses. The use of multiple software packages overcomes the shortcomings of each to provide a detailed simulation that can be used for sensitivity analyses and optimizations. In this paper, the framework was used to evaluate the performance of monoclonal antibody capture processes. To this end, the simulation framework incorporated dynamic models for the affinity chromatography step that were validated with experimental breakthrough curves. The results were integrated with an Intelligen SuperPro Designer process simulation for the evaluation of key performance indicators of the operations. As proof of concept, the framework was used to perform a sensitivity analysis and optimization for a case study in which we sought to compare membrane and resin chromatography for disposable and reusable batch capture platforms. Two membranes and one resin were selected for the capture media, which yielded six process alternatives to compare. The objective functions were set to be cost of goods, process time, and buffer utilization. The results of the optimization of these process alternatives were a set of operating conditions that display tradeoffs between competing objectives. From this application exercise, we conclude that the framework can handle multiple variables and objectives, and it is adaptable to platforms with different chromatography media and operating modes. Additionally, the framework is capable of providing ad hoc analyses for decision making in a specific production context.

Indexed as

Antibodies, MonoclonalSoftwareChromatography, AffinityComputer SimulationAntibodies, MonoclonalMembrane chromatographyMulti-objective optimizationSimulation-based optimizationSingle-use chromatography

Identifiers

PMID36586284
PMCPMC9868085
OpenAlexW4313379614

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.